A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247798



Internal ID20814838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178586299..178586917hg38UCSC Ensembl
chr1:178555434..178556052hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551363
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247798
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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